Adaptive Long‐Read Sequencing Reveals <scp>GGC</scp> Repeat Expansion in <scp><i>ZFHX3</i></scp> Associated with Spinocerebellar Ataxia Type 4

Zhongbo Chen(Institute of Human Genetics), Louis J. Ptáček(University of California, San Francisco), John Hardy(UK Dementia Research Institute), Pilar Álvarez Jerez(National Institute on Aging), Delia Gagliardi(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), David Pellerin(Montreal Neurological Institute and Hospital), Mina Ryten(Guy's Hospital), Clarissa Rocca(Institute of Human Genetics), Kylie Montgomery(Great Ormond Street Hospital), Claire Anderson(Great Ormond Street Hospital), Katherine D. Mathews(University of Iowa), Eleanor Self(Queen Mary University of London), Jasmaine Lee(Queen Mary University of London), Chris Clarkson(University of Cape Town), Hannah Macpherson(University College London), Emil K. Gustavsson(University of British Columbia), Cornelis Blauwendraat(National Institute of Neurological Disorders and Stroke), Henry Houlden(Queen Mary University of London), Arianna Tucci(Genomics England), Andrew Singleton(Short and Associates (United States)), Ying‐Hui Fu(University of California, San Francisco), James M. Polke(National Hospital for Neurology and Neurosurgery), Huihui Luo(Queen Mary University of London), Annarita Scardamaglia(Queen Mary University of London)
Movement Disorders
January 10, 2024
Cited by 49


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